Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.72008221T>C , CM000672.2:g.72008221T>C | GRCh38 |
| NC_000010.10:g.73767979T>C , CM000672.1:g.73767979T>C | GRCh37 |
| NC_000010.9:g.73437985T>C | NCBI36 |
| NG_012635.1:g.48860T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373115.5:c.1190T>C MANE Select | ENSP00000362207.4:p.Val397Ala | |
| ENST00000373115.4:c.1190T>C | ENSP00000362207.4:p.Val397Ala | |
| NM_004273.4:c.1190T>C | NP_004264.2:p.Val397Ala | |
| XM_006718075.2:c.1190T>C | XP_006718138.1:p.Val397Ala | |
| XM_011540369.1:c.1190T>C | XP_011538671.1:p.Val397Ala | |
| XM_006718075.4:c.1190T>C | XP_006718138.1:p.Val397Ala | |
| XM_011540369.2:c.1190T>C | XP_011538671.1:p.Val397Ala | |
| NM_004273.5:c.1190T>C MANE Select | NP_004264.2:p.Val397Ala |